Fresh Recalls

FDAClass II · Medical device · Recall Z-2311-2026 · Recalled June 17, 2026

Plum Solo Precision IV Pump recall — ICU Medical, Inc.

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Plum Solo Precision IV Pump
Company / brand
ICU Medical
Lot / serial / date codes
UDI-DI M335400011 Plum Solo Precision IV Pump v1.0.3
Distribution
Worldwide - US Nationwide distribution in the states of ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.
Agency product description and boundaries

Plum Solo Precision IV Pump, 40001-0401

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Plum Solo Precision IV Pump

3. Open the official notice or contact

Official recall ID
Z-2311-2026
Brand
ICU Medical
Classification
Class II
Units affected
13,613
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Lake Forest, IL, United States
Firm address
600 N Field Dr, N/A, 60045-4835

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI M335400011 Plum Solo Precision IV Pump v1.0.3
Distribution
Worldwide - US Nationwide distribution in the states of ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.
Firm notified the public via
Letter
FDA event ID
98872
Recall initiated
April 29, 2026
FDA classified
June 5, 2026
FDA report date
June 17, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 12:00 PM UTC. Record retrieved September 7, 2026 at 12:00 PM UTC.

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